Phenotype #0000128911

Individual ID 00163792
Associated disease CPDX2
Phenotype details several fetal form
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite CPDX-2
Age/Examination -
Age/Diagnosis 00y01m
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Fabienne Dufernez
Database submission license No license selected
Created by Fabienne Dufernez
Date created 2018-04-12 15:52:39 +02:00 (CEST)
Date last edited N/A

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